pain relief pm

Generic: acetaminophen, diphenhydramine hcl

Labeler: topco associates, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen, diphenhydramine hcl
Labeler topco associates, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
Topco Associates, LLC

Identifiers & Regulatory

Product NDC 36800-556
Product ID 36800-556_fb7880fb-a8fc-4276-aa2c-40d223988353
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2020-01-03

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36800556
Hyphenated Format 36800-556

Supplemental Identifiers

RxCUI
1092189
UPC
0036800327344
UNII
362O9ITL9D TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name pain relief pm (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-556-09) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-556-10) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

36800-556-09 1 BOTTLE, PLASTIC in 1 CARTON (36800-556-09) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC 36800-556-10 1 BOTTLE, PLASTIC in 1 CARTON (36800-556-10) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fb7880fb-a8fc-4276-aa2c-40d223988353", "openfda": {"upc": ["0036800327344"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["eaa98783-5800-4ae9-832f-f4a1fd1790fd"], "manufacturer_name": ["Topco Associates, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-556-09)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-556-09", "marketing_start_date": "20200103"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-556-10)  / 40 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-556-10", "marketing_start_date": "20200103"}], "brand_name": "Pain Relief PM", "product_id": "36800-556_fb7880fb-a8fc-4276-aa2c-40d223988353", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "36800-556", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Topco Associates, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200103", "listing_expiration_date": "20261231"}